Associate Director, Advertising and Promotional Compliance, US

About this role

The   Associate   Director, Advertising and Promotion Compliance, US   will serve as the Regulatory Affairs   (RA)   representative for   assigned products and therapeutic areas .    They will   be responsible   for   reviewing and approving the regulatory content of materials created for product promotion, disease   awareness   and public affairs communications. The   Associate   Director will also engage business partners for strategic planning on issues   pertaining to   product promotion and will   participate   in developing processes and procedures relevant to the creation,   review   and approval of promotional materials. The   Associate   Director   may   also act as the primary liaison with FDA on ad/promo regulatory issues concerning promotional   materials.

Accountabilities: • Reviewing   US promotional   and non-promotional/scientific   material, attending   review   meetings   and   providing   regulatory guidance to the cross-functional team responsible for ensuring   adherence to   global compliance standards and FDA regulations   pertaining to   prescription drug advertising,   promotion,   and communication   as applicable  

• Serv ing   as primary contact for communications with the Office of Prescription Drug Promotion (OPDP) and/or   Advertising and Promotional Labeling Branch (APLB) for assigned products, including responsibilities for the   timely   preparation and submission of promotional materials under cover of FDA Form 2253  

• As needed, provid ing   training support within Alexion on regulatory requirements for prescription drug promotion including, but not limited to, sales training and compliance training in preparation for scientific conferences  

• Providing   advice to product development teams on advertising and promotion issues to   facilitate   the strategic development of new products  

• Ensur ing   stakeholder   awareness of proposed and newly approved labeling changes   

• Inform ing , review ing   and provid ing   clear communication to all key stakeholders in both Promotional Review Committee (PRC) and Medical Review Committee (MRC) on planned label updates and how they may impact promotional and medical materials; provide key stakeholders with specific guidance on appropriate implementation of the label update, including ISI updates, for assigned therapeutic area in a timely manner

• Participates   in developing processes and procedures relevant to the creation, review and approval of advertising and promotional materials; develop best practices to   establish   standards and consistency across company products

• Maintains   regulatory   expertise   in product promotion compliance by keeping current with issued FDA enforcement actions and through attendance at relevant conferences and/or seminars .    Communicate new regulatory standards   pertaining to   prescription drug promotion to brand teams and management, as appropriate  

• Works  with management and cross-functional partners to analyze changes to the regulatory landscape and   determine   any internal impact and communicate and provide guidance to all impacted key stakeholders   

Essential Skills/Experience: • Bachelor’s Degree

• 5 years of relevant experience and/or relevant PharmD post-doctoral Fellowship experience

• Knowledge of U.S. advertising and promotional regulations

• Experience communicating and negotiating directly with OPDP and/or APLB

• Experience with global standards for advertising and promotion compliance

• Knowledgeable on industry compliance requirements and non-compliance examples and trends

• Experience with launching new products and/or new indication

• Solid understanding of business goals and common marketing concepts/tools, including the internet and social media

• Proficiency using promotional review software, such as Veeva Promomats and Veeva Medcomms 

Desirable Skills/Experience: • Advanced degree

• 7 years of relevant experience and/or relevant PharmD post-doctoral Fellowship experience

• History having direct reports or mentoring junior team members

• Proven track record practicing sound judgment as it relates to risk assessment

• Strong interpersonal, communication, and leadership skills

• Proven ability to prioritize and meet critical business timelines

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Joining Alexion means embracing an opportunity where work isn’t ordinary. We are a beacon in the global Biopharmaceutical landscape. Our closeness to patients brings us closer to our work and closer to each other. Combined with our brave, pioneering spirit – we are truly unique in R&D and healthcare. At Alexion, grow and innovate in a business with a rapidly expanding portfolio. Enjoy the vibe, entrepreneurial spirit, and autonomy of a leading biotech. You’ll join an energizing culture where people build connections to explore new ideas. As an important member of our commercial team, you'll be meeting the needs of some of the most under-served patients in the world. You will be empowered with tailored development programs designed not just for skill enhancement but for fostering a deep understanding of our patient's journeys. You’re supported by exceptional leaders ready to lift you in marketing, compliance, and beyond.

The annual base pay for this position ranges from $150,000 to $200,000 . Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified

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